H. Kitoh

发表

Delayed ossification of the proximal capital femoral epiphysis in Legg-Calvé-Perthes' disease.

H. Kitoh, T. Kitakoji, M. Katoh, 2003, The Journal of bone and joint surgery. British volume.

A recurrent mutation in type II collagen gene causes Legg-Calvé-Perthes disease in a Japanese family

H. Ohashi, Y. Miyamoto, S. Ikegawa, 2007, Human Genetics.

Lower limb pain following allogeneic hematopoietic stem cell transplantation in Japanese children.

Yoshiyuki Takahashi, N. Ishiguro, H. Kitoh, 2020, Journal of orthopaedic science : official journal of the Japanese Orthopaedic Association.

Is the timing of surgery associated with avascular necrosis after unstable slipped capital femoral epiphysis? A multicenter study.

Y. Iwamoto, H. Endo, H. Kitoh, 2017, Journal of orthopaedic science : official journal of the Japanese Orthopaedic Association.

Percutaneous pinning after prolonged skeletal traction with the hip in a flexed position for unstable slipped capital femoral epiphysis

N. Ishiguro, H. Kitoh, K. Mishima, 2017, Medicine.

Prediction of Clinically Significant Leg-Length Discrepancy in Congenital Disorders.

N. Ishiguro, H. Kitoh, Y. Nishida, 2015, Orthopedics.

Lansoprazole Upregulates Polyubiquitination of the TNF Receptor-Associated Factor 6 and Facilitates Runx2-mediated Osteoblastogenesis

A. Masuda, K. Ohno, Mikako Ito, 2015, EBioMedicine.

Transplantation of marrow-derived mesenchymal stem cells and platelet-rich plasma during distraction osteogenesis--a preliminary result of three cases.

N. Ishiguro, H. Kitoh, T. Kitakoji, 2004, Bone.

Corrective Osteotomy with an Original Plate for Moderate Slipped Capital Femoral Epiphysis

N. Ishiguro, H. Kitoh, T. Kitakoji, 2007 .

Early and late fracture following extensive limb lengthening in patients with achondroplasia and hypochondroplasia.

N. Ishiguro, H. Kitoh, Y. Nishida, 2014, The bone & joint journal.

Mutations in SIP1, encoding Smad interacting protein-1, cause a form of Hirschsprung disease

N. Nomura, T. Ono, Kanefusa Kato, 2001, Nature Genetics.

The effect of recombinant human bone morphogenetic protein-2 on the osteogenic potential of rat mesenchymal stem cells after several passages

N. Ishiguro, H. Kitoh, H. Ishikawa, 2007, Acta orthopaedica.

Osteogenic potential of rat mesenchymal stem cells after several passages.

N. Ishiguro, H. Kitoh, Fumiaki Sugiura, 2004, Biochemical and biophysical research communications.

Distraction Osteogenesis Enhanced by Osteoblastlike Cells and Collagen Gel

N. Ishiguro, H. Kitoh, T. Kitakoji, 2002, Clinical orthopaedics and related research.

FBN2, FBN1, TGFBR1, and TGFBR2 analyses in congenital contractural arachnodactyly

N. Matsumoto, H. Saitsu, T. Mizuguchi, 2007, American journal of medical genetics. Part A.

Comprehensive genetic analysis of relevant four genes in 49 patients with Marfan syndrome or Marfan‐related phenotypes

R. Fodde, T. Ogata, N. Matsumoto, 2006, American journal of medical genetics. Part A.

Activated FGFR3 prevents subchondral bone sclerosis during the development of osteoarthritis in transgenic mice with achondroplasia

N. Ishiguro, T. Seki, H. Kitoh, 2017, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

SPATIAL AND TEMPORAL DISTRIBUTION OF GROWTH FACTORS RECEPTORS IN THE CALLUS: IMPLICATIONS FOR IMPROVEMENT OF DISTRACTION OSTEOGENESIS

N. Ishiguro, H. Kitoh, K. Siwicka, 2011, Nagoya journal of medical science.

Mutations in the TGFβ binding-protein-like domain 5 of FBN1 are responsible for acromicric and geleophysic dysplasias.

D. Sillence, A. Munnich, J. Casanova, 2011, American journal of human genetics.

Platyspondylic lethal skeletal dysplasia, San Diego type, is caused by FGFR3 mutations.

W. Wilcox, S. Brodie, H. Kitoh, 1999, American journal of medical genetics.

The phenotypic spectrum of COL2A1 mutations

H. Ohashi, S. Ikegawa, N. Haga, 2005, Human mutation.

Novel and recurrent TRPV4 mutations and their association with distinct phenotypes within the TRPV4 dysplasia family

R. Hennekam, H. Tonoki, R. Hennekam, 2010, Journal of Medical Genetics.

Spondylo‐epiphyseal dysplasia, Maroteaux type (pseudo‐Morquio syndrome type 2), and parastremmatic dysplasia are caused by TRPV4 mutations

A. Mégarbané, T. Cho, S. Ikegawa, 2010, American journal of medical genetics. Part A.

Perhexiline maleate in the treatment of fibrodysplasia ossificans progressiva: an open-labeled clinical trial

K. Ohno, J. Horowitz, N. Ishiguro, 2013, Orphanet Journal of Rare Diseases.

Clinically applicable antianginal agents suppress osteoblastic transformation of myogenic cells and heterotopic ossifications in mice

A. Masuda, K. Ohno, Mikako Ito, 2012, Journal of Bone and Mineral Metabolism.

Congenital limb deficiency in Japan: a cross-sectional nationwide survey on its epidemiology

T. Ogata, N. Haga, H. Kitoh, 2018, BMC Musculoskeletal Disorders.

Extensive Bone Lengthening for a Patient with Linear Morphea

N. Ishiguro, H. Kitoh, K. Mishima, 2018, Case reports in orthopedics.

Meclozine Facilitates Proliferation and Differentiation of Chondrocytes by Attenuating Abnormally Activated FGFR3 Signaling in Achondroplasia

A. Masuda, K. Ohno, Mikako Ito, 2013, PloS one.

Extra pelvic ossification centers in thanatophoric dysplasia and platyspondylic lethal skeletal dysplasia-San Diego type

D. Rimoin, W. Wilcox, S. Brodie, 1998, Pediatric Radiology.

Advance Publication by J-STAGE Clinical Pediatric Endocrinology

K. Ozono, N. Haga, T. Kubota, 2021 .

Spondylometaphyseal dysplasia with cone‐rod dystrophy

Toshiyuki Yamamoto, M. Kondo, G. Nishimura, 2011, American journal of medical genetics. Part A.

Orthopaedic manifestations and diagnostic clues in children with Guillain–Barré syndrome

N. Ishiguro, H. Kitoh, T. Kitakoji, 2013, Journal of Children's Orthopaedics.

Novel COL9A3 mutation in a family with multiple epiphyseal dysplasia

R. Kosaki, H. Ohashi, S. Ikegawa, 2005, American journal of medical genetics. Part A.

Novel types of COMP mutations and genotype-phenotype association in pseudoachondroplasia and multiple epiphyseal dysplasia

Kozo Nakamura, N. Brunetti‐Pierri, H. Ohashi, 2002, Human Genetics.

Clinical Aspects and Current Therapeutic Approaches for FOP

H. Kitoh, 2020, Biomedicines.

Benign prenatal hypophosphatasia: a treatable disease not to be missed

Kanako Tachikawa, T. Michigami, N. Ishiguro, 2014, Pediatric Radiology.

Novel and recurrent mutations clustered in the von Willebrand factor A domain of MATN3 in multiple epiphyseal dysplasia

R. Kosaki, H. Ohashi, S. Ikegawa, 2004, Human mutation.

A simple bone cyst containing secretory cells in its lining membrane in a patient with polyostotic fibrous dysplasia

H. Kitoh, H. Nogami, 1999, Pediatric Radiology.

Characterisation of novel RUNX2 mutation with alanine tract expansion from Japanese cleidocranial dysplasia patient.

M. Kimura, N. Ishiguro, H. Kitoh, 2015, Mutagenesis.

C-type natriuretic peptide plasma levels are elevated in subjects with achondroplasia, hypochondroplasia, and thanatophoric dysplasia.

A. Aylsworth, E. Espiner, B. Zabel, 2015, Journal of Clinical Endocrinology and Metabolism.

Sagittal spinal alignment in patients with Legg‐Calve‐Perthes disease

N. Ishiguro, H. Kitoh, T. Kitakoji, 2007, Pediatrics international : official journal of the Japan Pediatric Society.

Molecular, radiologic, and histopathologic correlations in thanatophoric dysplasia.

D. Rimoin, L. Thompson, W. Wilcox, 1998, American journal of medical genetics.

Gain-of-Function of FGFR3 Accelerates Bone Repair Following Ischemic Osteonecrosis in Juvenile Mice

Y. Takegami, H. Kitoh, N. Kamiya, 2022, Calcified Tissue International.

Chronic lateral epiphyseal separation of the proximal tibia causes late-onset tibia vara.

N. Ishiguro, H. Kitoh, K. Mishima, 2018, Journal of pediatric orthopedics. Part B.

Novel Compound Heterozygous Mutations in the Cathepsin K Gene in Japanese Female Siblings with Pyknodysostosis

N. Ishiguro, H. Kitoh, K. Mishima, 2012, Molecular Syndromology.

Different genotype of periosteal and endosteal cells of a patient with polyostotic fibrous dysplasia

H. Kitoh, H. Nogami, Y. Yamada, 1999, Journal of medical genetics.

Efficacy of soluble lansoprazole-impregnated beta-tricalcium phosphate for bone regeneration

K. Ohno, H. Kitoh, S. Imagama, 2022, Scientific Reports.

Hyperpigmentation over the metacarpophalangeal joints and the malleoli in a case of hyaline fibromatosis syndrome with ANTXR2 mutations

M. Akiyama, H. Kitoh, K. Itomi, 2016, Journal of the European Academy of Dermatology and Venereology : JEADV.

Meclozine promotes longitudinal skeletal growth in transgenic mice with achondroplasia carrying a gain-of-function mutation in the FGFR3 gene.

K. Mori, A. Masuda, K. Ohno, 2015, Endocrinology.

A Mouse Distraction Osteogenesis Model.

H. Kitoh, H. Hibi, Y. Osawa, 2018, Journal of visualized experiments : JoVE.

Activated FGFR3 promotes bone formation via accelerating endochondral ossification in mouse model of distraction osteogenesis.

K. Ohno, N. Ishiguro, H. Kitoh, 2017, Bone.

Impact of fracture characteristics and disease-specific complications on health-related quality of life in osteogenesis imperfecta

K. Ozono, N. Haga, T. Kubota, 2019, Journal of Bone and Mineral Metabolism.

Effect of periosteal resection on longitudinal bone growth in a mouse model of achondroplasia

Y. Takegami, H. Kitoh, S. Imagama, 2020, Bone reports.

Physical, Mental, and Social Problems of Adolescent and Adult Patients with Achondroplasia

K. Ozono, N. Haga, T. Kubota, 2019, Calcified Tissue International.

Guided growth for coronal lower limb deformities in skeletal dysplasia

H. Kitoh, K. Mishima, M. Matsushita, 2022, Journal of pediatric orthopedics. Part B.

Disease-specific complications and multidisciplinary interventions in achondroplasia

H. Kitoh, K. Mishima, M. Matsushita, 2022, Journal of Bone and Mineral Metabolism.

Distraction Osteogenesis of the Lower Extremity in Patients With Achondroplasia/Hypochondroplasia Treated With Transplantation of Culture-Expanded Bone Marrow Cells and Platelet-Rich Plasma

N. Ishiguro, H. Kitoh, T. Kitakoji, 2007, Journal of pediatric orthopedics.

Clinical spectrum of fibroblast growth factor receptor mutations

E. Jabs, M. Passos-Bueno, W. Wilcox, 1999, Human mutation.

A retrospective comparative study of corrective osteotomy for tibial deformities with the multiaxial correction fixator and the circular fixator.

N. Ishiguro, H. Kitoh, K. Mishima, 2020, Journal of clinical orthopaedics and trauma.

A retrospective comparative study of corrective osteotomy for tibial deformities with the multiaxial correction ﬁ xator and the circular Journal of Clinical Orthopaedics and Trauma

H. Kitoh, K. Mishima, M. Matsushita, 2022 .

Differential Effects of Culture-expanded Bone Marrow Cells on the Regeneration of Bone Between the Femoral and the Tibial Lengthenings

N. Ishiguro, H. Kitoh, H. Kaneko, 2009, Journal of pediatric orthopedics.

Transplantation of culture expanded bone marrow cells and platelet rich plasma in distraction osteogenesis of the long bones.

Naoki Ishiguro, Hiroki Tsuchiya, N. Ishiguro, 2007, Bone.

Fibrodysplasia ossificans progressiva: Review and research activities in Japan

J. Kamizono, N. Haga, H. Kitoh, 2019, Pediatrics international : official journal of the Japan Pediatric Society.

SHOX nullizygosity and haploinsufficiency in a Japanese family: implication for the development of Turner skeletal features.

T. Ogata, G. Nishimura, H. Kitoh, 2002, The Journal of clinical endocrinology and metabolism.

A novel mutation of ALK2, L196P, found in the most benign case of fibrodysplasia ossificans progressiva activates BMP-specific intracellular signaling equivalent to a typical mutation, R206H.

Y. Okazaki, I. Owan, E. Jimi, 2011, Biochemical and biophysical research communications.

The effect of the platelet concentration in platelet-rich plasma gel on the regeneration of bone.

N. Ishiguro, H. Kitoh, K. Siwicka, 2008, The Journal of bone and joint surgery. British volume.

Biodistribution of locally or systemically transplanted osteoblast-like cells

T. Kondo, N. Ishiguro, H. Kitoh, 2014, Bone & joint research.

Multivariate Analyses of CT Findings in Typical Schizophrenia and Atypical Psychosis

H. Kitoh, T. Hayashi, T. Watanabe, 1992, The Japanese journal of psychiatry and neurology.

A Glutamine Repeat Variant of the RUNX2 Gene Causes Cleidocranial Dysplasia

N. Ishiguro, H. Kitoh, Y. Nishida, 2015, Molecular Syndromology.

A novel in-frame deletion of the RUNX2 gene causes a classic form of cleidocranial dysplasia

N. Ishiguro, H. Kitoh, Y. Tokita, 2013, Journal of Bone and Mineral Metabolism.

Skewed X-chromosome inactivation causes intra-familial phenotypic variation of an EBP mutation in a family with X-linked dominant chondrodysplasia punctata

N. Tanaka, H. Ohashi, S. Ikegawa, 2002, Human Genetics.

Isolated bifid rib: Clinical and radiological findings in children

N. Ishiguro, H. Kitoh, K. Mishima, 2012, Pediatrics international : official journal of the Japan Pediatric Society.

A novel NPR2 mutation (p.Arg388Gln) in a patient with acromesomelic dysplasia, type Maroteaux

G. Nishimura, H. Kitoh, T. Hasegawa, 2020, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Maternal administration of meclozine for the treatment of foramen magnum stenosis in transgenic mice with achondroplasia.

K. Ohno, N. Ishiguro, H. Kitoh, 2017, Journal of neurosurgery. Pediatrics.

Low bone mineral density in achondroplasia and hypochondroplasia

N. Ishiguro, H. Kitoh, Y. Nishida, 2016, Pediatrics international : official journal of the Japan Pediatric Society.

Meclozine Attenuates the MARK Pathway in Mammalian Chondrocytes and Ameliorates FGF2-Induced Bone Hyperossification in Larval Zebrafish

K. Ohno, Y. Hosono, H. Ebi, 2022, Frontiers in Cell and Developmental Biology.

Gene Mutations Responsible for Human Erythrocyte AMP Deaminase Deficiency in Poles

N. Nomura, H. Kitoh, Yasukazu Yamada, 1998 .

Mutations in PCYT1A, encoding a key regulator of phosphatidylcholine metabolism, cause spondylometaphyseal dysplasia with cone-rod dystrophy.

A. Moser, D. Valle, K. Doheny, 2014, American journal of human genetics.

Which Is a Better Method for Perthes’ Disease: Femoral Varus or Salter Osteotomy?

N. Ishiguro, H. Kitoh, T. Kitakoji, 2005, Clinical orthopaedics and related research.

Prediction of acetabular development after closed reduction by overhead traction in developmental dysplasia of the hip

N. Ishiguro, H. Kitoh, T. Kitakoji, 2006, Journal of orthopaedic science : official journal of the Japanese Orthopaedic Association.

Home traction in the treatment schedule of overhead traction for developmental dysplasia of the hip

N. Ishiguro, H. Kitoh, T. Kitakoji, 2005, Journal of orthopaedic science : official journal of the Japanese Orthopaedic Association.

A cross-sectional nationwide survey of osteosclerotic skeletal dysplasias in Japan.

H. Kitoh, K. Mishima, M. Matsushita, 2021, Journal of orthopaedic science : official journal of the Japanese Orthopaedic Association.

A case of mesomelic dysplasia Kantaputra type--new findings and a new diagnostic approach.

N. Ishiguro, H. Kitoh, K. Siwicka, 2008, Journal of pediatric orthopedics. Part B.

Deformity of the great toe in fibrodysplasia ossificans progressiva

Y. Iwamoto, J. Kamizono, N. Haga, 2010, Journal of orthopaedic science : official journal of the Japanese Orthopaedic Association.

Antley-Bixler syndrome: a disorder characterized by congenital synostosis of the elbow joint and the cranial suture.

T. Oki, Y. Tanaka, H. Kitoh, 1996, Journal of pediatric orthopedics.

Lys650Met substitution in the tyrosine kinase domain of the fibroblast growth factor receptor gene causes thanatophoric dysplasia Type I. Mutations in brief no. 199. Online.

W. Wilcox, S. Brodie, H. Kitoh, 1998, Human mutation.

Mutation in the gene encoding the fibroblast growth factor receptor‐3 in Korean children with achondroplasia

H. Kitoh, S. Yang, Yasukazu Yamada, 1998, Acta paediatrica Japonica : Overseas edition.

Chondrogenesis enhanced by overexpression of sox9 gene in mouse bone marrow-derived mesenchymal stem cells.

Naoki Ishiguro, Hiroki Tsuchiya, N. Ishiguro, 2003, Biochemical and biophysical research communications.

Y. Matsuyama, N. Ishiguro, H. Kitoh, 2011, European Spine Journal.

A RARE CASE OF FEMORAL HYPOPLASIA (PROXIMAL FOCAL FEMORAL DEFICIENCY) WITH OVERLAPPING PHENOTYPE OF MULLERIAN DUCT SYNDROME (MAYER-ROKITANSKY-HAUSER SYNDROME)

N. Vasan, H. Kitoh, Cheryl Melovitz‐Vasan, 2016 .

Predictive ability of inflammatory markers and laboratory parameters in Legg-Calvé-Perthes disease: A single-center retrospective comparative study.

H. Kitoh, S. Imagama, K. Mishima, 2022, Medicine.

Scurvy as a differential diagnosis of diffuse musculoskeletal pain in children: Two case reports

H. Kitoh, Akiko Kitamura, H. Kaneko, 2022, JOS Case Reports.

Mechanism of development of bronze baby syndrome in neonates treated with phototherapy.

H. Togari, K. Isobe, S. Onishi, 1982, Pediatrics.

Hyperuricemia cosegregating with osteogenesis imperfecta is associated with a mutation in GPATCH8

A. Masuda, K. Ohno, F. Rauch, 2011, Human Genetics.

Long-term Outcome of Gradual Reduction Using Overhead Traction for Developmental Dysplasia of the Hip Over 6 Months of Age

N. Ishiguro, H. Kitoh, K. Mishima, 2013, Journal of pediatric orthopedics.

Radiographic Analysis of Movements of the Acetabulum and the Femoral Head After Salter Innominate Osteotomy

N. Ishiguro, H. Kitoh, H. Kaneko, 2009, Journal of pediatric orthopedics.

Predictive Factors for Unsuccessful Treatment of Developmental Dysplasia of the Hip by the Pavlik Harness

N. Ishiguro, H. Kitoh, M. Kawasumi, 2009, Journal of pediatric orthopedics.

Tranilast stimulates endochondral ossification by upregulating SOX9 and RUNX2 promoters.

A. Masuda, K. Ohno, N. Ishiguro, 2016, Biochemical and biophysical research communications.

A Novel Heterozygous Mutation in the T-box Protein 4 Gene in an Adult Case of Small Patella Syndrome

T. Oda, H. Kitoh, Y. Ono, 2018, Journal of orthopaedic case reports.

A Histological and Ultrastructural Study of the Iliac Crest Apophysis in Legg-Calve-Perthes Disease

N. Ishiguro, H. Kitoh, T. Kitakoji, 2008, Journal of pediatric orthopedics.

Docking phenomenon and subsequent acetabular development after gradual reduction using overhead traction for developmental dysplasia of the hip over six months of age

H. Kitoh, T. Hattori, Akiko Kitamura, 2021, Journal of children's orthopaedics.

Appropriate Surgical Timing of Salter Innominate Osteotomy for Residual Acetabular Dysplasia in Children

H. Kitoh, T. Hattori, Akiko Kitamura, 2022, Journal of pediatric orthopedics.

A comparative study of blade plate fixation and external fixation in osteotomies for slipped capital femoral epiphysis

N. Ishiguro, H. Kitoh, T. Kitakoji, 2013, Journal of pediatric orthopedics. Part B.

Factors associated with an unfavourable outcome after Salter innominate osteotomy in patients with unilateral developmental dysplasia of the hip: does occult dysplasia of the contralateral hip affect the outcome?

N. Ishiguro, H. Kitoh, K. Mishima, 2014, The bone & joint journal.

Prognostic factors for trochanteric overgrowth after containment treatment in Legg–Calvé–Perthes disease

N. Ishiguro, H. Kitoh, K. Mishima, 2013, Journal of pediatric orthopedics. Part B.

A novel SOX9 H169Q mutation in a family with overlapping phenotype of mild campomelic dysplasia and small patella syndrome

G. Nishimura, N. Ishiguro, H. Kitoh, 2013, American journal of medical genetics. Part A.

Two children with hypophosphatasia with a heterozygous c.1559delT variant in the ALPL gene, the most common variant in Japanese populations

T. Ogi, H. Kitoh, Akiko Kitamura, 2022, Bone Reports.

Femoral lengthening with enzyme replacement therapy in an adolescent patient with prenatal benign hypophosphatasia: A case report.

H. Kitoh, Akiko Kitamura, H. Kaneko, 2021, Journal of orthopaedic science : official journal of the Japanese Orthopaedic Association.

Mutations in B3GALT6, which encodes a glycosaminoglycan linker region enzyme, cause a spectrum of skeletal and connective tissue disorders.

D. Chitayat, N. Matsumoto, Hironori Ito, 2013, American journal of human genetics.

Longitudinal study of the activities of daily living and quality of life in Japanese patients with fibrodysplasia ossificans progressiva

J. Toguchida, N. Haga, H. Kitoh, 2019, Disability and rehabilitation.

Radiographic characteristics of the hand and cervical spine in fibrodysplasia ossificans progressiva.

J. Kamizono, N. Haga, N. Ishiguro, 2014, Intractable & rare diseases research.

Patellar dislocation in achondroplasia

T. Oki, H. Kitoh, Y. Takamine, 2008, Journal of pediatric orthopedics. Part B.

Activated FGFR3 suppresses bone regeneration and bone mineralization in an ovariectomized mouse model

K. Ohno, H. Kitoh, B. Ohkawara, 2023, BMC Musculoskeletal Disorders.

Early radiographic risk factors for rigid relapse in idiopathic clubfoot treated with the Ponseti method.

N. Ishiguro, H. Kitoh, Y. Nishida, 2017, Foot and ankle surgery : official journal of the European Society of Foot and Ankle Surgeons.

The Biomechanical Effect of the Sensomotor Insole on a Pediatric Intoeing Gait

M. Inoue, N. Ishiguro, H. Kitoh, 2012, ISRN orthopedics.

K. Ozono, N. Haga, T. Kubota, 2021, Progress in rehabilitation medicine.

Thanatophoric dysplasia type I with syndactyly.

W. Wilcox, S. Brodie, H. Kitoh, 1998, American journal of medical genetics.

Identification of Mutations in the Gene Encoding the Fibroblast Growth Factor Receptor 3 in Japanese Patients with Achondroplasia

H. Kitoh, Yasukazu Yamada, H. Goto, 1995 .

[Molecular mechanism in the differentiation of chondrocytes].

N. Ishiguro, H. Kitoh, 2007, Clinical calcium.

Deformities of the elbow in achondroplasia.

H. Kitoh, T. Kitakoji, M. Katoh, 2002, The Journal of bone and joint surgery. British volume.

Comprehensive screening of multiple epiphyseal dysplasia mutations in Japanese population

R. Kosaki, H. Ohashi, S. Ikegawa, 2006, American journal of medical genetics. Part A.

Induction of systemic bone changes by preconditioning total body irradiation for bone marrow transplantation

G. Nishimura, H. Kitoh, Y. Shioda, 2008, Pediatric Radiology.

Inconvenience and adaptation in Japanese adult achondroplasia and hypochondroplasia: A cross-sectional study

K. Ozono, N. Haga, T. Kubota, 2021, Clinical Pediatric Endocrinology.

Early clinical and radiographic characteristics in fibrodysplasia ossificans progressiva: a report of two cases.

N. Ishiguro, H. Kitoh, T. Katagiri, 2011, The Journal of bone and joint surgery. American volume.

Chondroblastoma of the femoral neck as a cause of hip synovitis.

N. Ishiguro, H. Kitoh, Y. Nishida, 2012, Journal of pediatric orthopedics. Part B.

Characteristic calcaneal ossification: an additional early radiographic finding in infants with fibrodysplasia ossificans progressiva

E. Zackai, H. Kayserili, N. Haga, 2016, Pediatric Radiology.

Clinical dosage of meclozine promotes longitudinal bone growth, bone volume, and trabecular bone quality in transgenic mice with achondroplasia

K. Ohno, N. Ishiguro, H. Kitoh, 2017, Scientific Reports.

Treatment approaches for congenital transverse limb deficiency: Data analysis from an epidemiological national survey in Japan.

T. Ogata, N. Haga, H. Kitoh, 2020, Journal of orthopaedic science : official journal of the Japanese Orthopaedic Association.

Changes of the lower limb deformity in children with FGF23-related hypophosphatemic rickets treated with Burosumab: a single-center prospective study.

H. Kitoh, T. Hamajima, Akiko Kitamura, 2022, Journal of pediatric orthopedics. Part B.

Phase 1b study on the repurposing of meclizine hydrochloride for children with achondroplasia

Kazuki Nishida, H. Kitoh, S. Ueno, 2023, PLoS ONE.

Pharmacokinetics and safety after once and twice a day doses of meclizine hydrochloride administered to children with achondroplasia

N. Ishiguro, H. Kitoh, K. Mishima, 2020, PloS one.

Changes in the range of motion of the lower limb joints during extensive tibial lengthening in achondroplasia

N. Ishiguro, H. Kitoh, Koji Sato, 2018, Journal of pediatric orthopedics. Part B.

Meclozine ameliorates bone mineralization and growth plate structure in a mouse model of X‑linked hypophosphatemia

K. Ohno, T. Michigami, H. Kitoh, 2022, Experimental and therapeutic medicine.

A case of severe proximal focal femoral deficiency with overlapping phenotypes of Al-Awadi-Raas-Rothschild syndrome and Fuhrmann syndrome

N. Ishiguro, H. Kitoh, Y. Nishida, 2014, Pediatric Radiology.

Prognostic factors for mobility in children with osteogenesis imperfecta.

H. Kitoh, T. Hattori, Akiko Kitamura, 2022, Medicine.

Spondylo‐epiphyseal dysplasia, Maroteaux type (pseudo‐Morquio syndrome type 2), and parastremmatic dysplasia are caused by TRPV4 mutations

A. Mégarbané, T. Cho, S. Ikegawa, 2010, American journal of medical genetics. Part A.

Mutations in the TGFβ binding-protein-like domain 5 of FBN1 are responsible for acromicric and geleophysic dysplasias.

D. Sillence, A. Munnich, J. Casanova, 2011, American journal of human genetics.

Comparison of surgical and nonsurgical containment methods for patients with Legg-Calvé-Perthes disease of the onset ages between 6.0 and 8.0 years: Salter osteotomy versus a non-weight-bearing hip flexion-abduction brace

N. Ishiguro, H. Kitoh, K. Mishima, 2019, Journal of pediatric orthopedics. Part B.

Long-term oral meclozine administration improves survival rate and spinal canal stenosis during postnatal growth in a mouse model of achondroplasia in both sexes

Y. Takegami, H. Kitoh, B. Ohkawara, 2024, JBMR plus.

A Common Mutation in the Tyrosine Kinase Domain of the Fibroblast Growth Factor Receptor 3 Gene in Two Japanese Patients with Hypochondroplasia

H. Kitoh, Yasukazu Yamada, H. Goto, 1996 .